5-(5-Aryl-1,3,4-oxadiazole-2-carbonyl)furan-3-carboxylate and new cyclic C-glycoside analogues from carbohydrate precursors with MAO-B, antimicrobial and antifungal activities.

Cyclization of acyclic C-glycoside derivatives 1a,b to 2a,b as the major isomers, and 4a,b as the minor isomers were carried out. The isopropylidene derivatives 3a,b were prepared, as well as the hydrazide derivative 6, which was condensed with a variety of aldehydes to give hydrazones 7a-e which were also prepared from the compounds 12a-e. Acetylation of 7a,d gave the corresponding acetyl derivatives 8a,d, respectively. In addition, the dicarbonyl compound 9 was prepared in the hydrate form, which reacted with a number of aroylhydrazines to give the corresponding bisaroylhydrazones 10a-d, which were cyclized into 1,3,4-oxadiazoles 11a-d. Furthermore, two of the prepared compounds were examined to show the ability to activate MAO-B. In addition a number of prepared compounds showed antibacterial and antiviral activities.

1. Introduction

C-glycosides have received a great deal of attention from the synthesis and medicinal chemistry community, due to their increased stability to hydrolysis as well as their presence in a number of interesting natural products [1]. Furthermore, heterocyclic compounds containing the five-membered oxadiazole nucleus possess a diversity of useful biological effects. Substituted n class="Chemical">1,3,4-oxadiazoles are of considerable pharmaceutical interest, for instance, 2-amino-1,3,4-oxadiazoles act as muscle relaxants [2] and show antimitotic activity. Anti-inflammatory [3,4], antimicrobial [4], anti-hepatitis B [5] and anti-diarrheal activity [6] of some new 1,3,4-oxadiazole derivatives was also reported. Recently several 1,3,4-oxadiazole derivatives were identified as potentially active antimycobacterial [7,8], antitubercular [9], anticonvulsant [10] and anticancer [11] agents, and also reported as enzyme tyrosinase inhibitors [12]. In light of these interesting biological activities, it became interested in synthesizing some new C-glycosides of substituted 1,3,4-oxadiazole derivatives and evaluating their antimicrobial potential.

2. Results and Discussion

2.1. Chemistry

It has been shown [13] that the acid-catalysed, intramolecular dehydration of 1b using conc. n class="Chemical">HCl (0 °C) yields a mixture of a major D-ribo anhydro isomer 2b (with inversion of configuration), and a minor D-arabino-anhydro isomer 4b (with retention of configuration). On the other hand, the dehydration of 1a with aqueous acetic acid (10%) under reflux [14], afforded a mixture of anhydro derivatives 2a (major isomer) and 4a (the minor one) and in addition, a mixture of 2b and 4b were obtained from 1b using aqueous acetic acid (10%). The minor isomer 4a could be isolated as a solid.

The anomeric configurations [15] of these anhydro derivatives were ascertained from the n class="Chemical">1H-NMR spectra of their isopropylidene derivatives 3a,b which were prepared by an improved procedure [16] through treatment of the crude anhydro derivatives with acetone in the presence of catalytic amount of p-toluenesulphonic acid (see Experimental and Scheme 1).

Scheme 1

Synthesis of isopropylidene derivatives 3a,b.

1H-NMR spectra (n class="Chemical">CDCl3) of compounds 3a,b displayed the two methyl protons signals of the 2,2-dimethyldioxolane ring at δ (1.544–1.352) having Δδ 0.187. The signals of the sugar protons of these isopropylidene derivatives were assigned from the 2D 1H-NMR spectrum of compound 3b (Figure 1), and the characteristic chemical shifts as compared with those reported for anhydro analogues [16], whereby the C-1' proton appears as a singlet at δ 5.00 (J1',2' = 0.00 Hz). Confirmation of the anomeric configuration of the isopropylidene derivatives 3a,b can be obtained from the zero coupling constant value (J1',2' = 0.00 Hz), which is an unequivocal [16,17] proof for the trans arrangement of the H-1' and H-2' (β-D-configuration) as well as from the Δδ value (0.187) [15,18,19]. Boiling of the crude 2b,4b mixture with hydrazine hydrate resulted in the formation of 6, which upon condensation with a number of aldehydes afforded the corresponding anhydrohydrazone derivatives 7a–e which were also obtained as only one isomer (inversion of configuration at C-1') by boiling the compounds 12a–e [20,21] with aqueous acetic acid under reflux. The assignment of the signals for the sugar protons in the 1H-NMR spectra of compounds 7a–e were based on the 2D 1H-NMR spectrum of compound 7e. In addition, acetylation of the anhydrohydrazones 7a,d afforded the corresponding O-acetyl derivatives 8a,d, respectively (see Experimental and Scheme 2).

Figure 1

2D 1H-NMR spectrum of compound 3b.

Scheme 2

Synthesis of carbohydrazone derivatives.

Periodate oxidation [22] of the prepared anhydro-derivatives 2b,4b, gave the corresponding n class="Chemical">dialdehyde in the hemialdal structure 9 [22,23]. Furthermore, condensation of dialdehyde 9 with two molar equivalents of aroylhydrazines, afforded the corresponding bisaroylhydrazones 10a–d. 1H-NMR spectra of compounds 10a–d (DMSO-d6), showed the two (NH) protons at δ (11.78–11.55) as two singlets, followed by the aromatic protons as a multiplet at δ (7.82–7.00), two (CH=N) as a doublet at 7.9 for H(2) and a multiplet at 7.7 for H(1), and the proton at position-4 in the furan ring as a singlet at 6.7 ppm. The methine proton was shown as a doublet at δ 5.1, followed by a multiplet at 4.1 ppm for the protons of the two methylene groups. Oxidative cyclization of the prepared bisaroylhydrazones 10a–d and a physical and chemical study of the oxidation products, revealed that their properties could not be reconciled with that of 1,2,3-triazole derivatives C [24,25,26,27] but rather was compatible with that of 1,3,4-oxadiazole derivatives 11a–d, that were obtained in appropriate yields. Infrared spectra of these compounds showed no enol benzoate group as expected for the 1,2,3-triazole derivatives C, and showed instead a band at 1,667–1,660 cm−1, which was attributed to the conjugated carbonyl group of compounds 11a–d (see Experimental and Scheme 3 and Scheme 4).

Scheme 3

Synthesis of bisaroylhydrazone derivatives 10a–d.

Scheme 4

Synthesis of 1,3,4-oxadiazole derivatives 11a–d.

Furthermore, 1H-NMR spectra (n class="Chemical">CDCl3) of these products showed the disappearance of signals corresponding to two (NH) and two (CH=N), methine and methylene protons. Indeed, it is noteworthy that the integration of the aromatic part (δ 8.22–7.36 ppm), referred to one aromatic ring only, in accord with structures 11a,b,d. In addtion, these oxidative cyclization products displayed the proton at position-4 in the furan ring as the most downfield signal at δ (8.49–8.48) ppm; this proton resonated at a lower field region than that expected in CDCl3, which may be attributed to the electron withdrawing effect of the carbonyl group on the neighboring carbon atom, as well as conjugation with the phenyl oxadiazole moiety. In addition, the structure of the oxidation products 11a–d was further supported through their boiling with hydrochloric acid, which didn’t afford the corresponding amine derivatives D as expected from 1,2,3-triazole derivatives (see Experimental part and Scheme 4). Moreover, the proposed mechanism for formation of 11a–d may proceed via elimination of one aroylhydrazone part (oxidation in presence of iodine and mercuric oxide) due to the bulkiness of the molecule, followed by oxidative cyclization of the other aroylhydrazone part to afford compounds 11a–d (Scheme 5).

Scheme 5

Proposed mechanism for formation of ethyl 2-methyl-5-(5-aryl-1,3,4-oxadiazole-2-carbonyl)furan-3-carboxylate.

2.2. Pharmacological Screening

2.2.1. MAO-B Activity

2.2.1.1. Effect of Tested Compounds on MAO-B

This study aimed to evaluate the effect of two selected newly prepared compounds 7c,e on MAO-B activity given the biological importance of MAO-B [28,29,30,31,32,33,34,35,36,37,38].

2.2.1.2. Determination of Vmax and Km

TheVmax and Km of the MAO-B catalyzed reaction in the presence or absence of each exn class="Chemical">amined compound was carried out by plotting V against [S], each separately. The obtained results revealed that MAO-B was activated in the presence of compounds 7c and 7e, each separately, by 6.57- and 6.97-fold, respectively. In addition, the MAO-B catalyzed reactions in the presence of compounds 7c and 7e have Vmax equal to 0.49 and 0.71, respectively. Meanwhile the Km values were 1.72 and 1.32, respectively. Our obtained data showed that compound 7e was an effective MAO-B activator, which increases the affinity of substrate to bind with the active site of MAO-B enzyme. That may be attributed to the presence of highly conjugated system with the cinamyl group in 7e as compared with bulky furan ring in 7c (Table 1, Figure 2).

Table 1

Effect of substrate concentration on the rate of MAO-B catalyzed reactions in presence of the examined compounds 7c and 7e, compared to control.

Substrate conc.	Rate
	Control	7c	7e
0.25 × 10−3	0.020	0.068	0.222
0.50 × 10−3	0.042	0.085	0.240
1.00 × 10−3	0.050	0.151	0.315
1.50 × 10−3	0.180	0.250	0.363
2.00 × 10−3	0.200	0.322	0.440
3.00 × 10−3	0.280	0.430	0.560
4.00 × 10−3	0.365	0.481	0.674
5.00 × 10−3	0.380	0.498	0.700

Figure 2

Effect of substrate concentration on the rate of MAO-B catalyzed reactions in the presence of the examined compounds 7c,e compared to control.

Effect of substrate concentn class="Species">ration on the rate of MAO-B catalyzed reactions in presence of the examined compounds 7c and 7e, compared to control.

Effect of substrate concentn class="Species">ration on the rate of MAO-B catalyzed reactions in the presence of the examined compounds 7c,e compared to control.

2.2.2. Antibacterial and Antifungal Activities

The compounds 3b, 6, 7c,e, 10a–c and 11a,b,d have been studied for their antibacterial and antifungal activities against four bacterial species (Escherichia coli, n class="Species">Bacillus sp., Staphylococcus sp., and Sarcina sp.) and six fungal species (Aspergillus niger, Aspergillus fmigatus, Alternaria sp., Fusarium sp., Chaetomium sp., and Penicillium sp.) using the Nutrient Agar (NA) and Sabouraud Dextrose Agar (SDA) diffusion methods, respectively, in DMSO solvent (Table 2).

Table 2

Inhibition zones of tested compounds against selected microorganisms (mm).

Compound No.	Bacteria
	Gram positive			Gram negative
	Bacillus sp.	Sarcina sp.	Staphylococcus sp.	E. coli
3b	….	….	….	….
6	….	….	2	….
7c	….	….	0.5	….
7e	….	….	2	….
10a	….	….	….	….
10b	….	….	….	….
10c	….	….	….	….
11a	….	….	1	….
11b	….	….	….	….
11d	….	….	….	….
Compound No.	Fungi
	Aspergillus niger	Aspergillus fumigatus	Alternaria sp.	Fusarium sp.	Chaetomium sp.	Penicilliu sp.
3b	1	1	….	2	….	….
6	….	….	1	1	2	2
7c	1	1	0.5	2	….	0.5
7e	….	2.5	0.5	2	….	1
10a	….	….	….	….	….	….
10b	1	….	….	….	….	….
10c	1	….	….	….	….	….
11a	0.5	….	0.5	….	….	2
11b	….	….	….	….	….	….
11d	….	….	….	2	….	….

….: No effect.

It was found that they were active against Gram positive bacteria (Staphylococcus sp.). In addition, the replacement of the bulky n class="Chemical">furan ring in compound 7c by the cinamyl group in compound 7e, increased the antibacterial activity against Gram positive bacteria (Staphylococcus sp.), due to the conjugation caused by the cinamyl group [39]. With respect to antifungal activity, the compounds 3b, 6, 7c,e, and 11a were found to be generally active against the tested fungi.

3. Experimental

3.1. Chemistry

Melting points were determined with a Melt-temp. apparatus and are uncorrected. TLC was performed on Baker-Flex n class="Chemical">silica gel 1B-F plates and the spots were detected by UV light absorption. IR spectra were recorded on Perkin Elmer. USA Spectrometer. 1H-NMR, 13C-NMR, and 2D 1H-NMR were recorded on a JEOL JNM ECA 500 MHz instrument using tetramethylsilane as an internal standard. Mass spectra were recorded on GCMS solution DI Analysis Shimadzu Qp-2010 Plus. Optical rotation was obtained at 22 °C with a Perkin-Elmer Model 241 Polarimeter 10 cm, 1 mL microcell. Microanalyses were performed at the faculty of Science, Cairo University, Cairo, Egypt. Solutions were evaporated under diminished pressure unless otherwise stated. The ChemDraw-Ultra-8.0 has been used in generating the nomenclature of the prepared compounds.

3.1.1. Ethyl 5-(2',3'-Dihydroxytetrahydrofuran-1'-yl)-2-methylfuran-3-carboxylates 2b,4b

Compound 1b (15.0 g, 54.74 mmol) was boiled under reflux with aqueous acetic acid (300 mL, 10%) for 5 h, while the reaction was monitored by TLC (n class="Chemical">chloroform-methanol, 20:1, V/V), the starting material disappeared and a more mobile spot (Rf: 0.5) was obtained. The solvent was evaporated under diminished pressure and washed with toluene (3 times, 10 mL each) to obtain 2b as a yellow thick syrup along with a solid mass of 4b. Separation of 4b from the syrup was carried out by washing the mixture with ethanol where it was partially soluble in ethanol on cold; the overall yield was 69.7%; the solid mass was recrystallized from ethanol as colourless needles; IR (KBr): 3,426 (OH), 1,712 cm−1 (CO-ester).

3.1.2. Synthesis of Isopropylidene Derivatives

General Methods. A solution of 2a,4a[22] or 2b,4b mixture (4.42 mmol) in dry acetone (100 mL) was treated with n class="Chemical">p-toluenesulphonic acid (10.98 mmol) and stirred at room temperature. The reaction mixture was monitored by TLC (hexane-ethyl acetate, 7:1, V/V), the starting material disappeared after 7 h and a more mobile spot appeared. The mixture was then poured onto a saturated solution of sodium bicarbonate, extracted with chloroform, the organic layer washed with water and dried over anhydrous sodium sulphate. Evaporation of the dried filtrate gave pale yellow needles.

1-[5-(2',3'-O-Isopropylidene-β- (3a). Yield 51%; recrystallized from ethanol as colourless needles, mp 97–99 °C; Rf: 0.35 (hexane-ethyl acetate, 7:1, V/V), IR (KBr): 1,682 (CO-acetyl), 1,604, 1,571 cm−1 (C=C); 1H-NMR (CDCl3); δ: 1.358, 1.544 (2s, 6H, CMe2, Δδ 0.187), 2.376 (s, 3H, COCH3), 2.559 (s, 3H, CH3(furan)), 3.909 (dd, 1H, H-4'a, J3',4'a = 3.85 Hz, J4'b,4'a = 10.70 Hz), 4.049 (d, 1H, H-4'b, J4'b,4'a = 10.70 Hz), 4.892–4.937 (m, 2H, H-2', H-3'), 5.001 (s, 1H, H-1'), 6.475 (s, 1H, CHfuran); MS: m/z (%), 267 (3.50, M++1), 266 (4.82, M+), 137 (36.26), 125 (21.36), 111 (35.32), 109 (21.18), 99 (21.56), 97 (52.51), 95 (33.70), 85 (46.86), 83 (49.75), 81 (32.98), 73 (26.34), 71 (66.24), 69 (61.30), 67 (23.40), 60 (25.40), 57 (100), 56 (21.33), 55 (65.29).

Ethyl 5-(2',3'-O-isopropylidene-β- (3b). Yield (90%); recrystallized from ethanol as colourless needles, mp 70–72 °C; Rf: 0.63 (hexane-ethyl acetate, 7:1, V/V); [a] −69.03; IR (KBr): 1,709 (CO-ester) 1,613, 1,583 cm−1 (C=C); 1H-NMR (CDCl3); δ: 1.324 (t, 3H, CH3(ester), J = 6.90 Hz), 1.352, 1.538 (2s, 6H, CMe2, Δδ 0.187), 2.542 (s, 3H, CH3(furan)), 3.870 (dd, 1H, H-4'a, J3',4'a = 3.80 Hz, J4'b,4'a = 10.70 Hz), 4.029 (d, 1H, H-4'b, J4'b,4'a = 10.70 Hz), 4.260 (q, 2H, CH2(ester), J = 6.90 Hz), 4.876–4.928 (m, 2H, H-2', H-3'), 5.003 (s, 1H, H-1'), 6.486 (s, 1H, CHfuran); MS: m/z (%), 297 (6.3, M++1), 296 (20.6, M+), 182 (100), 181 (30.6), 145 (60), 153 (43), 137 (25), 136 (25.6), 105 (21.3), 80 (27.5), 79 (28.8), 69 (38.1), 65 (28.8), 60 (13.8), 59 (76.3), 56 (25), 55 (30.6), 53 (33.8), 52 (44.4), 51 (60), 50 (25).

5-(2',3'-Dihydroxytetrahydrofuran-1'-yl)-2-methylfuran-3-carbohydrazide (6). A solution of 2b,4b (2.0 g, 7.81 mmol) in n class="Chemical">ethanol (10 mL) was treated with hydrazine hydrate (4 mL) under reflux for one hour, while the reaction was monitored by TLC (chloroform-methanol, 6:1, V/V) which revealed the absence of the starting material and formation of two more mobile spots, Rf: 0.49 (major) and 0.74 (minor). After cooling 6 separated out, was filtered off, washed with a little ethanol, and dried; yield 65%. It was recrystallized from ethanol as colourless needles, mp 185–187 °C. TLC showed one spot only, Rf: 0.49 (chloroform-methanol, 6:1, V/V); The minor isomer was left in the mother liquor; [a] −58.98; IR (KBr): 3,384, 3,314 (OH and NH2), 3272 (NH), 1,636 cm−1 (CO-amide); 1H-NMR (DMSO-d6); δ: 2.463 (s, 3H, CH3(furan)), 3.570 (dd, 1H, H-4'b, J3',4'b = 2.30 Hz, J4'b,4'a = 9.15 Hz), 3.979 (dd, 1H, H-4'a, J3',4'a = 4.60 Hz, J4'b,4'a = 9.15 Hz), 4.029–4.066 (m, 2H, H-3', H-2'), 4.312 (s, 2H, NH2), 4.395 (d, 1H, H-1', J1',2' = 6.90 Hz), 4.985 (d, 1H, 2'-OH, J2',OH = 4.60 Hz), 5.076 (d, 1H, 3'-OH, J3',OH = 6.85 Hz), 6.715 (s, 1H, CHfuran), 9.243 (s, 1H, NH). After shaking with D2O, the NH, NH2, and the two hydroxyl protons disappeared; MS: m/z (%), 243 (2.19, M++1), 242 (16.89, M+), 224 (0.47, M+-H2O), 212 (11.54, M+-2NH), 211 (100, M+-NHNH2); Anal. Calcd for C10H14N2O5: C, 49.58; H, 5.84; N, 1.55%; found: C, 49.58; H, 5.83; N, 1.56%.

3.1.3. Reactions of 6 with a Number of Aldehydes

General Methods

Method A. A solution of 6 (0.5 g, 2.066 mmol) in ethanol (5 mL) containing acetic acid (0.1 mL) was treated with the corresponding aldehyde (2.066 mmol), and the reaction mixture was refluxed on water bath for 10 min. After cooling the product 3-carbohydrazone derivative that separated out, was filtered off, washed with little ethanol, and dried.

Method B. A solution of (1',2',3',4'-tetrahydroxybutyl)furan-3-carbohydrazone 12a–e [20,21] (4.799 mmol) was refluxed with aqueous acetic acid (10%) for 5 h. After cooling the compounds 7a–e that separated out as a crystalline mass were filtered off, washed with little ethanol, and dried.

5-(2',3'-Dihydroxytetrahydron class="Chemical">furan-1'-yl)-2-methyl-N-[(2-phenyl-2H-1,2,3-triazol-4-yl)methyl-ene]furan-3-carbohydrazone (7a). Yield of method A 87%; recrystallized from ethanol as colourless needles, mp 209–210 °C; Rf: 0.39 (chloroform-methanol, 15:1, V/V); [a] −37.59; IR (KBr): 3,395 (OH), 3,108 (NH), 1,669 (CO-amide), 1,638 cm−1 (C=N); 1H-NMR (DMSO-d6); δ: 2.524 (s, 3H, CH3(furan)), 3.616 (dd, 1H, H-4'b, J3',4'b = 2.30 Hz, J4'b,4'a = 9.20 Hz), 4.008–4.026 (m, 1H, H-4'a), 4.036–4.095 (m, 2H, H-3', H-2'), 4.493 (d, 1H, H-1', J1',2' = 6.90 Hz), 5.043 (ss, 1H, 2'-OH), 5.142 (d, 1H, 3'-OH, J3',OH = 6.15 Hz), 6.860 (s, 1H, CHfuran), phenyl protons: 7.432 (t, 1H,p-H), 7.568 (t, 2H, O-H), 8.017 (d, 2H, m-H), 8.401 (s, 1H, CH=N), 8.537 (s, 1H, CHtriazole), 11.610 (s, 1H, NH). After shaking with D2O, the NH proton and the two hydroxyl protons disappeared; MS: m/z (%), 399 (0.89, M++2), 398 (5.36, M++1), 397 (23.99, M+), 379 (3.55, M+-H2O), 324 (21.85), 253 (11.94, M+-phenyltriazole moiety), 211 (100), 137 (35.81), 77 (20.56, C6H5); Anal. Calcd for C19H19N5O5: C, 57.42; H, 4.80; N, 17.64%; found: C, 57.43; H, 4.82; N, 17.62%.

N-[(2-(p-Bromophenyl)-2H-1,2,3-triazol-4-yl)methylene]-5-(2',3'-dihydroxyn class="Species">tetrahydrofuran-1'-yl)-2-methylfuran-3-carbohydrazone (7b). Yield of method A 84%; recrystallized from ethanol as colourless needles, mp 241–243 °C; Rf: 0.38 (chloroform-methanol, 15:1, V/V); [a] −31.39; IR (KBr): 3,423 (OH), 3,249 (NH), 1,653 (CO-amide), 1,618 cm−1 (C=N); 1H-NMR (DMSO-d6); δ: 2.519 (s, 3H, CH3(furan)), 3.617 (dd, 1H, H-4'b, J3',4'b = 2.30 Hz, J4'b,4'a = 9.95 Hz), 4.019 (dd, 1H, H-4'a, J3',4'a = 3.85 Hz, J4'b,4'a = 9.95 Hz), 4.080–4.109 (m, 2H, H-3', H-2'), 4.493 (d, 1H, H-1', J1',2' = 6.90 Hz), 5.051 (ss, 1H, 2'-OH), 5.147 (d, 1H, 3'-OH, J3',OH = 6.10 Hz), 6.857 (s, 1H, CHfuran), p-bromophenyl protons: 7.752 (d, 2H, m-H), 7.954 (d, 2H, o-H), 8.422 (s, 1H, CH=N), 8.518 (s, 1H, CH(triazole)), 11.630 (s, 1H, NH). After shaking with D2O, the NH proton and the two hydroxyl protons disappeared; 13C-NMR; δ: 14.00 (C-13), 70.91 (C-4'), 73.32 (C-3'), 75.33 (C-2'), 76.50 (C-1'), 107.79 (C-12), 115.11 (C-11), 120.92 (C-10), 121.23 (C-9), 133.27 (C-8), 135.16 (C-7), 137.74 (C-6), 138.52 (C-5), 146.50 (C-4), 151.71 (C-3), 158.19 (C-2), 159.84 (C-1); MS: m/z (%), 478/476 (2.03, 2.17, M++1), 477/475 (8.85, 9.10, M+), 459/457 (1.25, 1.24, M+-H2O), 253 (10.01, M+-p-bromophenyl triazole moiety), 211 (100), 137 (34); Anal. Calcd for C19H18BrN5O5: C, 47.90; H, 3.83; N, 14.71; Br, 16.77%; found: C, 47.91; H, 3.81; N, 14.70; Br, 16.78%.

Ethyl 5-[(2-(5-(2',3'-dihydroxytetrahydrofuran-1'-yl)-2-methylfuran-3-carbonyl)hydrazono)-methyl]-2-methylfuran-3-carboxylate (7c). Yield of method A 93%; [a] −44.42; IR (KBr): 3,426 (OH), 3,208 (NH), 1,694 (CO-ester), 1,655 (CO-amide), 1,616 cm−1 (C=N); 1H-NMR (DMSO-d6); δ: 1.254 (t, 3H, CH3(ester), J = 7.65 Hz), 2.501 (s, 3H, CH3(furan-1)), 2.580 (s, 3H, CH3(furan-2)), 3.603 (dd, 1H, H-4'b, J3',4'b = 2.30 Hz, J4'b,4'a = 9.90 Hz), 4.004 (dd, 1H, H-4'a, J3',4'a = 4.60 Hz, J4'b,4'a = 9.90 Hz), 4.043–4.088 (m, 2H, H-3', H-2'), 4.209 (q, 2H, CH2(ester), J = 7.65 Hz), 4.467 (d, 1H, H-1', J1',2' = 6.85 Hz), 5.028 (d, 1H, 2'-OH, J2',OH = 3.80 Hz), 5.124 (d, 1H, 3'-OH, J3',OH = 6.10 Hz), 6.830 (s, 1H, CHfuran-1), 7.059 (s, 1H, CHfuran-2), 8.150 (s, 1H, CH=N), 11.409 (s, 1H, NH). After shaking with D2O, the NH proton and the two hydroxyl protons disappeared; MS: m/z (%), 408 (0.79, M++2), 407 (4.16, M++1), 406 (18.26, M+), 211 (100), 154 (32.75); Anal. Calcd for C19H22N2O8: C, 56.13; H, 5.47; N, 6.86%; found: C, 56.15; H, 5.46; N, 6.89%.

N-Benzylidene-5-(2',3'-dihydroxytetrahydrofuran-1'-yl)-2-methylfuran-3-carbohydrazone (7d). Yield of method A 84%; recrystallized from n class="Chemical">ethanol as colourless needles, mp 86–88 °C; Rf: 0.345 (chloroform-methanol, 15:1, V/V); [a] −42.16; IR (KBr): 3,380 (OH and NH), 1,661 (CO-amide), 1,616 cm−1 (C=N); 1H-NMR (DMSO-d6); δ: 2.513 (s, 3H, CH3(furan)), 3.608 (dd, 1H, H-4'b, J3',4'b = 2.30 Hz, J4'b,4'a = 9.95 Hz), 4.012 (dd, 1H, H-4'a, J3',4'a = 4.60 Hz, J4'b,4'a = 9.95 Hz), 4.065–4.089 (m, 2H, H-3', H-2'), 4.476 (d, 1H, H-1', J1',2' = 6.90 Hz), 5.043 (d, 1H, 2'-OH, J2',OH = 3.85 Hz), 5.141 (d, 1H, 3'-OH, J3',OH = 6.10 Hz), 6.869 (s, 1H, CH(furan)), phenyl protons: 7.395–7.436 (m, 3H, p-H, O-H), 7.672 (d, 2H, m-H), 8.340 (s, 1H, CH=N), 11.389 (s, 1H, NH). After addition of D2O, the NH proton and the two hydroxyl protons disappeared; MS: m/z (%), 331 (2.25, M++1), 330 (10.80, M+), 227 (9.18, M+-C6H5CN), 211 (100), 154 (59.63), 77 (9.32, C6H5); Anal. Calcd for C17H18N2O5: C, 61.80; H, 5.50; N, 8.45%; found: C, 61.8; H, 5.49; N, 8.48%.

5-(2',3'-Dihydroxytetrahydrofuran-1'-yl)-2-methyl-N-(3-phenylallylidene)furan-3-carbohydrazone (7e). Yield of method A 92.5%; recrystallized from ethanol as colourless needles, mp 162–163 °C; Rf: 0.78 (chloroform:-methanol, 10:1, V/V); [a] −42.55; IR (KBr): 3,409 (OH), 3,241 (NH), 1,657 (CO-amide), 1,628 cm−1 (C=N); 1H-NMR (DMSO-d6); δ: 2.499 (s, 3H, CH3(furan)), 3.598–3.617 (m, 1H, H-4'b), 4.013 (dd, 1H, H-4'a, J3',4'a = 3.80 Hz, J4'b,4'a = 9.90 Hz), 4.026–4.104 (m, 2H, H-3', H-2'), 4.476 (d, 1H, H-1', J1',2' = 6.90 Hz), 5.025 (d, 1H, 2'-OH, J2',OH = 3.80 Hz), 5.121 (d, 1H, 3'-OH, J3',OH = 6.15 Hz); 6.849 (s, 1H,CHfuran), 7.00 (bs, 2H, CH=CH), phenyl protons: 7.273–7.302 (m, 1H, p-H), 7.355 (t, 2H, O-H), 7.585 (d, 2H, m-H); 8.124 (d, 1H, CH=N, J = 6.15 Hz), 11.264 (s, 1H, NH); MS: m/z (%), 358 (0.21, M++2), 357 (0.95, M++1), 356 (3.22, M+), 338 (0.11, M+-H2O), 320 (0.21, M+-2H2O), 279 (0.52, M+-C6H5), 211 (100), 154 (55.50), 130 (35.56), 77 (8.65, C6H5), 43 (49, COCH3); Anal. Calcd for C19H20N2O5: C, 64.03; H, 5.64; N, 7.84%; found: C, 64.04; H, 5.66; N, 7.86%.

3.1.4. Reactions of Compounds 7a,d with Acetic Anhydride

General Method: A solution of the sugar derivative 7n class="Species">a or 7d (1.51 mmol) in a mixture of pyridine (15 mL) and acetic anhydride (15 mL) was kept overnight at room temperature with occasional shaking. Then it was poured onto crushed ice, the di-O-acetyl derivative that separated out, was filtered off, washed with water, and dried.

1'-[2-Methyl-3-(2-((2-phenyl-2H-1,2,3-triazol-4-yl)methylene)hydrazinecarbonyl)furan-5-yl]-tetra-hydrofuran-2',3'-diyl diacetate (8a). Yield 76.5%; recrystallized from dilute ethanol as colourless needles, mp 179–181 °C; Rf 0.5 (hexane-ethyl acetate, 2:1, V/V); [a] −47.75; IR (KBr): 3,217 (NH), 1,754 (OAc), 1,647 (CO-amide), 1,601 cm−1 (C=N); 1H-NMR (CDCl3); δ: 2.061, 2.139 (2s, 6H, 2OAc), 2.677 (s, 3H, CH3(furan)), 3.984–3.968 (m, 1H, H-4'b), 4.371 (dd, 1H, H-4'a, J3',4'a = 4.60 Hz, J4'b,4'a = 9.95 Hz), 4.925 (d, 1H, H-1', J1',2' = 6.10 Hz), 5.492–5.532 (m, 2H, H-3', H-2'), 6.744 (bs, 1H, CHfuran), 7.462–7.478 (m, 1H, p-H), 7.531–7.625 (m, 2H, O-H), 8.019–8.141 (m, 4H, m-H, CH=N, CHtriazole), and 12.239 (s, 1H, NH); MS: m/z (%), 482 (0.61, M++1), 481 (1.97, M+), 363 (22.58), 362 (100), 295 (67.47), 137 (21.53), 115 (19.79), 77 (15.78); Anal. Calcd for C23H23N5O7: C, 57.35; H, 4.82; N, 14.53%; found: C, 57.38; H, 4.82; N, 14.55%.

1'-[3-(2-Benzylidenehydrazinecarbonyl)-2-methylfuran-5-yl]tetrahydrofuran-2',3'-diyl diacetate (8d). Yield 80%; recrystallized from dilute n class="Chemical">methanol as colourless needles, mp 81–82 °C; Rf 0.5 (hexane-ethyl acetate, 2:1, V/V); [a] −48.37; IR (KBr): 3,248 (NH), 1,752 (OAc), 1,654 (CO-amide), 1,582 cm−1 (C=N); 1H-NMR (CDCl3); δ: 2.070, 2.125 (2s, 6H, 2OAc), 2.602 (s, 3H, CH3(furan)), 3.954–3.974 (m, 1H, H-4'b), 4.381–4.350 (m, 1H, H-4'a), 4.950 (bs, 1H, H-1'), 5.417–5.524 (m, 2H, H-3', H-2'), 6.620 (s, 1H, CHfuran), 7.519–7.549 (m, 5H, phenyl protons), 7.883 (d, 1H, CH=N, J = 7.65 Hz), 9.550 (s, 1H, NH); MS: m/z (%), 415 (0.39, M++1), 414 (0.81, M+), 295 (100), 77 (2.61); Anal. Calcd for C21H22N2O7: C, 60.86; H, 5.37; N, 6.77%; found: C, 60.86; H, 5.35; N, 6.76%.

Ethyl 5-(3,5-dihydroxy-1,4-dioxan-2-yl)-2-methylfuran-3-carboxylate (9). A solution of 2b,4b mixture (12.96 g, 50.62 mmol) in distilled water (20 mL) was treated dropwise with a solution of sodium metaperiodate (10.825 g, 50.62 mmol) in distilled water (20 mL) with continuous stirring for 3 h. The dialdehyde that separated out was filtered off, washed with little water, and dried, yield 67%; Rf: 0.38 (chloroform-methanol, 15:1, V/V). Recrystallized from ethanol as colourless needles, mp 111–113 °C (Lit. [22], 111–113 °C); IR (KBr): 3,426 (OH), 1,712 cm−1 (CO-ester); 1H-NMR (CDCl3); δ: 1.293–1.326 (m, 3H, CH3(ester)), 2.519 (s, 3H, CH3(furan)), 3.380–3.428 (m, 1H, H-6b), 3.745–3.947 (m, 1H, H-6a), 4.222–4.387 (m, 2H, 3-OH, 5-OH), 4.275 (q, 2H, CH2(ester)), 4.609–4.745 (m, 1H, H-5), 5.112–5.125 (m, 1H, H-3), 5.514–5.534 (m, 1H, H-2), and 6.677 (s, 1H, CHfuran).

3.1.5. Reactions of 9 with a Number of Aroylhydrazines

General Method: A solution of 9 (2.0 g, 7.353 mmol) in ethanol (10 mL) containing acetic acid (0.1 mL) was treated with the corresponding aroylhydrazine (14.71 mmol) in ethanol (10 mL). The reaction mixture was refluxed on water bath for 15 min, the bisaroylhydrazone derivative that separated out was filtered off, washed with little ethanol, and dried.

Ethyl 5-[2-(2-benzoylhydrazono)-1-(2-(2-benzoylhydrazono)ethoxy)ethyl]-2-methylfuran-3-carboxylate (10a). Yield 61%; recrystallized from n class="Chemical">ethanol-chloroform as colourless needles, mp 204–206° C; Rf: 0.55 (chloroform-methanol, 10:1, V/V); IR (KBr): 3,280, 3,197 (2NH), 1,715 (CO-ester), 1,658 (CO-amide), 1,591 cm−1 (C=N); 1H-NMR (DMSO-d6); δ: 1.223 (t, 3H, CH3(ester), J = 6.90 Hz ), 2.524 (s, 3H, CH3(furan)), 4.086–4.199 (m, 4H, CH2, CH2(ester)), 5.150 (d, 1H, CH, J = 6.85 Hz), 6.736 (s, 1H, CHfuran), phenyl protons: 7.472–7.476 (m, 4H, O-H), 7.550–7.546 (m, 2H, p-H), 7.794–7.837 (m, 4H, m-H), 7.719 (bs, 1H, CH=N1), 7.912 (d, 1H, CH=N2, J = 6.10 Hz), 11.673 (s, 1H, NH3), 11.777 (s, 1H, NH4); MS: m/z (%), 472 (0.57, M+-H2O), 354 (56.88), 181 (31.16), 173 (29.44), 153 (23.60), 147 (93.31), 121 (41.45), 106 (49.34), 105 (100), 104 (23.78), 78 (21.08), 77 (99.13), 51 (77.47), 50 (24.02); Anal. Calcd for C26H26N4O6: C, 63.65; H, 5.35; N, 11.43%; found: C, 63.66; H, 5.34; N, 11.42%.

Ethyl 5-[2-(2-(p-toluoyl)hydrazono)-1-(2-(2-(p-toluoyl)hydrazono)ethoxy)ethyl]-2-methylfuran-3-carboxylate (10b). Yield 58%; recrystallized from ethanol-chloroform as colourless needles, mp 204–206 °C; Rf: 0.22 (chloroform-methanol, 15:1, V/V); IR (KBr): 3,305, 3,183 (2NH), 1,717 (CO-ester), 1,651 (CO-amide), 1,625, 1,612 cm−1 (C=N); 1H-NMR (DMSO-d6); δ: 1.222 (t, 3H, CH3(ester), J = 6.85 Hz), 2.327 (s, 6H, 2CH3(toluoyl)), 2.522 (s, 3H, CH3(furan)), 4.103–4.196 (m, 4H, CH2, CH2(ester)), 5.132 (d, 1H, CH, J = 6.90 Hz), 6.727 (s, 1H, CHfuran), aromatic protons: 7.265–7.280 (m, 4H, O-H), 7.708–7.747(m, 5H, m-H, CH=N1), 7.899 (d, 1H, CH=N2, J = 6.10 Hz), 11.601 (s, 1H, NH3), 11.716 (s, 1H, NH4); MS: m/z (%), 518 (0.09, M+), 500 (0.18, M+-H2O), 368 (31.86), 161 (44.53), 161 (44.53), 119 (100), 91 (50.53), 65 (19.49); Anal. Calcd for C28H30N4O6: C, 64.87; H, 5.85; N, 10.78%; found: C, 64.85; H, 5.83; N, 10.80%.

Ethyl 5-[2-(2-(p-anisoyl)hydrazono)-1-(2-(2-(p-anisoyl)hydrazono)ethoxy)ethyl]-2-methylfuran-3-carboxylate (10c). Yield 57%; recrystallized from ethanol-chloroform as colourless needles, mp 204–206 °C; Rf: 0.32 (chloroform:-methanol, 10:1, V/V); IR (KBr): 3,268, 3,212 (2NH), 1,718 (CO-ester), 1,645 (CO-amide), 1,610 cm−1 (C=N); 1H-NMR (DMSO-d6); δ: 1.225 (t, 3H, CH3(ester), J = 6.15 Hz), 2.525 (s, 3H, CH3(furan)), 3.776 (s, 6H, 2OCH3), 4.156–4.199 (m, 4H, CH2, CH2(ester)), 5.127 (d, 1H, CH, J = 6.15 Hz), 6.726 (s, 1H, CHfuran), aromatic protons: 6.700–7.008 (m, 4H, m-H), 7.799–7.837 (m, 4H, O-H), 7.707 (bs, 1H, CH=N1), 7.895 (d, 1H, CH=N2, J = 6.10 Hz), 11.554 (s, 1H, NH3), 11.653 (s, 1H, NH4); MS: m/z (%), 532 (0.15, M+-H2O), 135 (100); Anal. Calcd for C28H30N4O8: C, 61.05; H, 5.47; N, 10.19%; found: C, 61.08; H, 5.49; N, 10.18%.

Ethyl 5-[2-(2-(p-chlorobenzoyl)hydrazono)-1-(2-(2-(p-chlorobenzoyl)hydrazono)ethoxy)ethyl]-2-methylfuran-3-carboxylate (10d). Yield 62%; recrystallized from ethanol-chloroform as colourless needles, mp 204–206 °C; Rf: 0.4 (chloroform-methanol, 15:1, V/V); IR (KBr): 3,270, 3,215 (2NH), 1,719 (CO-ester), 1,650 (CO-amide), 1,612 cm−1 (C=N); Anal. Calcd for C26H24Cl2N4O6: C, 55.80; H, 4.33; N, 10.02; Cl, 12.69%; found: C, 55.82; H, 4.32; N, 10.02; Cl, 12.68%.

3.1.6. Reactions of Compounds 10a–d with Yellow Mercuric Oxide

General Method: A solution of 10a–d (4.5 mmol) in dry ether (50 mL) was stirred with yellow n class="Chemical">mercuric oxide (3.0 g), magnesium oxide (0.3 g), and iodine (2.5 g) at room temperature for 48 h under anhydrous condition. The reaction mixture was filtered off, and the filtrate washed with potassium iodide solution, sodium thiosulphate, and water, respectively, then dried over anhydrous sodium sulphate. On evaporation of the dried filtrate a yellow syrup was obtained, which was crystallized from ethanol. An additional crop was obtained by extracting the inorganic residue with chloroform which upon concentration and dilution with ethanol yielded the same product.

Ethyl 2-methyl-5-(5-phenyl-1,3,4-oxadiazole-2-carbonyl)furan-3-carboxylate (11a). Yield 36%; recrystallized from ethanol as colourless needles, mp 168–170 °C; Rf: 0.41 (hexane-ethyl acetate, 6:1, V/V); IR (KBr): 1,715 (CO-ester), 1,660 (C=O), 1,594 cm−1 (C=N); 1H-NMR (CDCl3); δ: 1.391 (t, 3H, CH3(ester), J = 6.85 Hz), 2.778 (s, 3H, CH3(furan)), 4.344 (q, 2H, CH2(ester), J = 6.85 Hz), phenyl protons: 7.565 (t, 2H, O-H), 7.611-7.637 (m, 1H, p-H), 8.210-8.224 (m, 2H, m-H), 8.491 (s, 1H, CHfuran); MS: m/z (%), 328 (3.07, M++2), 327 (20.48, M++1), 326 (100, M+), 181 (22.15), 153 (32.73), 145 (61.44), 77 (49.04); Anal. Calcd for C17H14N2O5: C, 62.57; H, 4.32; N, 8.59%; found: C, 62.57; H, 4.33; N, 8.60%.

Ethyl 2-methyl-5-(5-(p-tolyl)-1,3,4-oxadiazole-2-carbonyl)furan-3-carboxylate (11b). Yield 39%; recrystallized from ethanol as colourless needles, mp 185–187 °C; Rf: 0.52 (hexane-ethyl acetate, 6:1, V/V); IR (KBr): 1,715 (CO-ester), 1,660 (C=O), 1,611 cm−1 (C=N); 1H-NMR (CDCl3); δ: 1.390 (t, 3H, CH3(ester), J = 6.90 Hz), 2.457 (s, 3H, CH3(tolyl)), 2.775 (s, 3H, CH3(furan)), 4.348 (q, 2H, CH2(ester), J = 6.90 Hz), phenyl protons: 7.361 (d, 2H, O-H), 8.098 (d, 2H, m-H), 8.482 (s, 1H, CHfuran); Anal. Calcd for C18H16N2O5: C, 63.53; H, 4.76; N, 8.25%; found: C, 63.52; H, 4.74; N, 8.23%.

Ethyl 2-methyl-5-[5-(p-anisyl)-1,3,4-oxadiazole-2-carbonyl]furan-3-carboxylate (11c). Yield 21%; recrystallized from ethanol as colourless needles, mp 182–183 °C; Rf: 0.41 (hexane-ethyl acetate, 6:1, V/V); IR (KBr): 1,714 (CO-ester), 1,657 (C=O), 1,606 cm−1 (C=N); Anal. Calcd for C18H16N2O6: C, 60.66; H, 4.55; N, 7.86%; found: C, 60.67; H, 4.53; N, 7.86%.

Ethyl 2-methyl-5-[5-(p-chlorophenyl)-1,3,4-oxadiazole-2-carbonyl]furan-3-carboxylate (11d). Yield 39%; recrystallized from ethanol as colourless needles, mp 177–178 °C; Rf: 0.59 (hexane-ethyl acetate, 6:1, V/V); IR (KBr): 1,723 (CO-ester), 1,667 (C=O), and 1,600 cm−1 (C=N); 1H-NMR (CDCl3); δ: 1.391 (t, 3H, CH3(ester), J = 6.85 Hz), 2.778 (s, 3H, CH3(furan)), 4.353 (q, 2H, CH2(ester), J = 6.85 Hz), p-chlorophenyl protons: 7.550 (d, 2H, m-H), 8.158 (d, 2H, O-H), 8.482 (s, 1H, CHfuran); 1H-NMR (DMSO-d6); δ: 1.293 (t, 3H, CH3(ester), J = 6.85 Hz), 2.692 (s, 3H, CH3(furan)), 4.269 (q, 2H, CH2(ester), J = 6.85 Hz), p-chlorophenyl protons: 7.700 (d, 2H, m-H), 8.082 (d, 2H,O-H), 8.170 (s, 1H, CHfuran); MS: m/z (%), 362/360 (100, 42, M+), 181 (78.7), 179 (71.29), 153 (78.02), 141/139 (11.12, 33.56), 137 (39.6), 113/111 (10.89, 33.86); Anal. Calcd for C17H13ClN2O5: C, 56.62; H, 3.64; N, 7.75; Cl, 9.81%; found: C, 56.60; H, 3.63; N, 7.77; Cl, 9.83%.

3.2. Pharmacological Screening

3.2.1. MAO-B Activity

3.2.1.1. Enzyme Preparation

Rabbit n class="Chemical">brain was homogenized in 9 volumes of ice-cold 0.1 M sodium phosphate buffer (pH 7.4) with an Ultra-Turrax 18/2 homogenizer. The separated mitochondrial fraction was suspended in phosphate buffer to give a final volume of 1 mL g−1 weight of tissue [40].

3.2.1.2. Enzyme Assay

Monoamine oxidase-B activity was assayed in presence and absence of the exn class="Chemical">amined compounds each separately using benzylamine as substrate by continuous recording on a Pye Unicam SP8-100 Double Beam Spectrophotometer of the increase in extinction at 250 nm produced at 38 °C.

3.2.1.3. Determination of Vmax and Km

The Vmax and Km of MAO-B catalyzed reaction in presence or absence of each exn class="Chemical">amined compound 7c and 7e was carried out by plotting the rate of the reaction (V) against substrate concentration [S], each separately.

3.2.2. Antibacterial and Antifungal Screening

The antibacterial and antifungal activities of synthesized compounds 3b, 6, 7c,e, 10a–c and 11a,b,d against four bacterial species (Escherichia coli, n class="Species">Bacillus sp., Staphylococcus sp., and Sarcina sp.) and six fungal species (Aspergillus niger, Aspergillus fmigatus, Alternaria sp., Fusarium sp., Chaetomium sp., and Penicillium sp.). have been studied by using the Nutrient Agar (NA) and Sabouraud Dextrose Agar (SDA) diffusion methods, respectively in DMSO solvent. The bacteria were subcultured on Nutrient Agar medium (NA), whereas, fungi were subcultured on Sabouraud Dextrose Agar (SDA). The composition is given in g/L unless otherwise stated. The pH value of the media was adjusted to 7 ± 0.1 prior to sterilization with 0.1 M sodium hydroxide or hydrochloric acid. All media were prepared with distilled water and sterilized by autoclaving at 121 °C for 20 min. Nutrient Agar (NB): Peptone, 5; beef extract, 3; NaCl, 5; agar, 20. Sabouraud Dextrose Agar (SDA): Peptone, 10; glucose, 40; agar, 20. The stock solutions (1 mg/mL) of the test chemicals were prepared by dissolving 10 mg of the test compounds in 10 mL dimethylsulphoxide (DMSO) solvent. Petri plates (150 mm × 15 mm) were prepared by pouring 60 mL of SDA and allowed to solidify. Plates were dried and 1 mL of each standardized inoculums suspension was poured and uniformly spread. The excess inoculums was drained and the inoculums was allowed to dry for 15 min. Eight equidistant wells were made in the medium using a sterile cork borer (6 mm in diameter and 50 μL of the test chemicals (1 mg/mL) diluted in DMSO 2% were placed into the wells. The Petri-dishes containing bacterial and fungi species were incubated at 37 °C for 24 h, and 48 h, respectively. The tests were carried in triplicate. The antimicrobial activity was measured as the diameter (mm) of clear zone of growth inhibition.

4. Conclusions

Some new C-glycoside derivatives and heterocyclic derivatives of n class="Chemical">carbohydrate have been prepared and their physical and biological properties were studied. It was found that compounds with highly conjugated systems are acting as MAO-B activators, as well as antibacterial agents, meanwhile all tested compounds have antifungal activities.